US7214798B2 - Derivatives of piperidinyl-and piperazinyl-alkyl carbamates, preparation methods thereof and application of same in therapeutics - Google Patents

Derivatives of piperidinyl-and piperazinyl-alkyl carbamates, preparation methods thereof and application of same in therapeutics Download PDF

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US7214798B2
US7214798B2 US11/262,211 US26221105A US7214798B2 US 7214798 B2 US7214798 B2 US 7214798B2 US 26221105 A US26221105 A US 26221105A US 7214798 B2 US7214798 B2 US 7214798B2
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group
mmol
alkyl
piperidyl
conh
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US20060089344A1 (en
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Ahmed Abouabdellah
Philippe Burnier
Christian Hoornaert
Jean Jeunesse
Frederic Puech
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Sanofi Aventis France
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Sanofi Aventis France
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Priority to US13/229,106 priority patent/US20120004207A1/en
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    • C07D401/14—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing three or more hetero rings
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
    • C07D413/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings
    • C07D413/04—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings directly linked by a ring-member-to-ring-member bond
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D417/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
    • C07D417/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings
    • C07D417/04—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings directly linked by a ring-member-to-ring-member bond
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D471/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
    • C07D471/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
    • C07D471/04—Ortho-condensed systems
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D491/00—Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00
    • C07D491/02—Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00 in which the condensed system contains two hetero rings
    • C07D491/04—Ortho-condensed systems
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D495/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having sulfur atoms as the only ring hetero atoms
    • C07D495/02—Heterocyclic compounds containing in the condensed system at least one hetero ring having sulfur atoms as the only ring hetero atoms in which the condensed system contains two hetero rings
    • C07D495/04—Ortho-condensed systems

Definitions

  • the invention relates to piperidyl- and piperazinyl-alkylcarbamate derivatives and to the preparation and therapeutic application thereof.
  • a first subgroup of compounds consists of compounds for which:
  • a subject of the invention is also, among the compounds of general formula (I), compounds corresponding to the general formula (I′):
  • the compounds of general formula (I) may comprise one or more asymmetric carbons. They may exist in the form of enantiomers or diastereoisomers. These enantiomers and diastereoisomers, and also mixtures thereof, including racemic mixtures, form part of the invention.
  • the compounds of general formula (I) may exist in the form of bases or of acid-addition salts. Such addition salts form part of the invention.
  • salts are advantageously prepared with pharmaceutically acceptable acids, but the salts of other acids that are useful, for example, for the purification or isolation of the compounds of formula (I) also form part of the invention.
  • the compounds of general formula (I) may be in the form of hydrates or solvates, i.e. in the form of associations or combinations with one or more water molecules or with a solvent. Such hydrates and solvates also form part of the invention.
  • the compounds of the invention may be prepared according to various methods, illustrated by the schemes that follow.
  • a first method (Scheme 1) consists in reacting an amine of general formula (II), in which A, B, R 1 , n and m are as defined above, with a carbonate of general formula (IIIa) in which Z represents a hydrogen atom or a nitro group, R 4 is as defined above and R represents a methyl or ethyl group.
  • the carbamate ester of general formula (Ia) thus obtained is then converted into a compound of general formula (I), via aminolysis using an amine of general formula R 5 NH 2 in which R 5 is as defined above.
  • the aminolysis reaction may be performed in a solvent such as methanol or a mixture of solvents such as methanol and tetrahydrofuran or methanol and dioxane.
  • One variant for obtaining the compounds of general formula (I) (Scheme 1) consists in reacting an amine of general formula (II), as defined above, with a carbonate of general formula (IIIb), in which Z represents a hydrogen atom or a nitro group and R 4 and R 5 are as defined above, in a solvent such as toluene or dichloroethane, at a temperature of between 0° C. and 80° C.
  • the carbonates of general formula (IIIa) and (IIIb) may be prepared according to any method described in the literature, for example by reacting an alcohol of general formula HOCHR 4 COOR, in which R represents a methyl or ethyl group, or HOCHR 4 CONHR 5 in which R 4 and R 5 are as defined above, with phenyl chloroformate or 4-nitrophenyl chloroformate, in the presence of a base such as triethylamine or diisopropylethylamine.
  • a base such as triethylamine or diisopropylethylamine.
  • a second method for obtaining the compounds of general formula (I) (Scheme 2) consists in reacting a derivative of general formula (IIa) in which Y represents a hydroxyl, mesylate or tosylate group or a chlorine, bromine or iodine atom and A, B, R 1 , n and m are as defined above, with an oxazolidinedione of general formula (IV) in which R 4 is as defined above, to give the oxazolidinedione derivative of general formula (V).
  • the reaction may be performed according to the Mitsunobu conditions (Synthesis, 1981, 1–28), for example via the action of diethyl or diisopropyl azodicarboxylate in the presence of triphenylphosphine.
  • the reaction may be performed in the presence of a base such as 1,1,3,3-tetramethylguanidine, sodium hydride or sodium tert-butoxide in a solvent such as tetrahydrofuran, acetonitrile or dimethylformamide, at a temperature of between 0° C.
  • the compounds of general formulae (I), (Ia), (II), (IIa) and (V), in which R 1 is substituted with a group R′′ may also be prepared by reacting the corresponding compounds of general formulae (I), (Ia), (II), (IIa) and (V), for which R 1 is substituted with a chlorine, bromine or iodine atom or with a triflate group in the position into which the group R′′ is to be introduced, with an aryl- or heteroaryl-boronic acid derivative according to the Suzuki reaction conditions (Chem. Rev. 1995, 95, 2457–2483) or with an aryl- or heteroaryl-trialkylstannane derivative according to the Stille reaction conditions (Angew. Chem. Int. Ed. 1986, 25, 504–524).
  • the amines of general formula R 5 NH 2 are commercially available.
  • a subject of the invention is also the compounds of formula (Ia) in which n, m, A, B, R 1 and R 4 are as defined above and R represents a methyl or ethyl group.
  • the compounds of formula (Ia) are useful as synthetic intermediates for the preparation of the compounds of formula (I).
  • a subject of the invention is also the compounds of formula (V) in which n, m, A, B, R 1 and R 4 are as defined above, the following compounds being excluded:
  • the compounds of formula (V) are useful as synthetic intermediates for the preparation of the compounds of formula (I).
  • m.p. (° C.) represents the melting point in degrees Celsius.
  • the mixture is allowed to cool to room temperature and is concentrated under reduced pressure.
  • the residue is taken up in ethyl acetate and water, the aqueous phase is separated out and extracted three times with ethyl acetate, and the combined organic phases are washed with saturated aqueous sodium chloride solution and dried over sodium sulfate. After evaporating off the solvent, the residue obtained is purified by chromatography on silica gel, eluting with a 40/60 mixture of ethyl acetate and cyclohexane.
  • the mixture is allowed to cool to room temperature, the insoluble material is separated out by filtration and the filtrate is concentrated under reduced pressure.
  • the residue is taken up in 20 ml of ether and stirred at room temperature for 20 minutes.
  • the insoluble material is again separated out and the filtrate is concentrated under reduced pressure.
  • the residue obtained is purified by chromatography on silica gel, eluting with a 90/10/1 mixture of dichloromethane, methanol and 28% aqueous ammonia.
  • the salt formed is separated out and the filtrate is concentrated under reduced pressure.
  • the residue obtained is purified by chromatography on silica gel, eluting with a 97/3 mixture of dichloromethane and methanol. An oily residue is obtained, which is taken up with a solution of hydrochloric acid (5N) in isopropanol. The mixture is concentrated to dryness and the salt obtained is then recrystallized from a 1/1 mixture of acetone and diisopropyl ether.
  • the salts are separated out by filtration through Celite and the filtrate is then concentrated under reduced pressure.
  • the residue is taken up in ethyl acetate and water, the aqueous phase is separated out and extracted twice with ethyl acetate, and the combined organic phases are washed with saturated aqueous sodium chloride solution and dried over sodium sulfate. After evaporating off the solvent, the residue obtained is purified by chromatography on silica gel, eluting with a 97/3 mixture of dichloromethane and methanol.
  • the mixture is concentrated to dryness under reduced pressure.
  • the residue is taken up in 40 ml of dichloromethane and 30 ml of aqueous sodium hydroxide solution (1M).
  • the aqueous phase is separated out and extracted twice with dichloromethane, the combined organic phases are washed with saturated aqueous sodium chloride solution and dried over sodium sulfate, and the filtrate is concentrated under reduced pressure. 2.70 g of product are obtained in the form of a brown paste, which is used without further purification in the following step.
  • 0.63 g (9.57 mmol) of potassium cyanide is added portionwise to a suspension of 2.63 g (9.57 mmol) of 1-[4-(2-chloroethyl)-1-piperidyl]isoquinoline, prepared in step 2.2, and 0.048 g (0.29 mmol) of potassium iodide in 30 ml of dimethyl sulfoxide.
  • the reaction mixture is maintained at about 120° C. for 16 hours.
  • the mixture is allowed to cool to room temperature and 90 ml of water and ethyl acetate are then added.
  • the aqueous phase is separated out and extracted three times with ethyl acetate, the combined organic phases are washed with saturated aqueous sodium chloride solution and dried over sodium sulfate, and the filtrate is concentrated under reduced pressure.
  • the residue thus obtained is purified by chromatography on silica gel, eluting with a 30/70 mixture of ethyl acetate and cyclohexane.
  • reaction medium is cooled to about 0° C. and 15 ml of aqueous sodium hydroxide solution (1M) are then added slowly.
  • the mixture is stirred at room temperature for 30 minutes, followed by portionwise addition of wet sodium sulfate.
  • the salts are separated out by filtration through paper and the phases are then allowed to separate by settling.
  • the aqueous phase is extracted three times with ethyl acetate, the combined organic phases are dried over sodium sulfate and the filtrate is concentrated under reduced pressure.
  • the residue thus obtained is purified by chromatography on silica gel, eluting with a 93/7/0.7 mixture of dichloromethane, methanol and 28% aqueous ammonia.
  • Example 1 The process is performed as in Example 1 (step 1.4). Starting with 0.350 g (1.30 mmol) of 3-[1-(1-isoquinolyl)-4-piperidyl]propanamine, obtained in step 2.4, and 0.32 g (1.43 mmol) of ethyl[(phenyloxycarbonyl)oxy]acetate, prepared in step 1.3 of Example 1, and after chromatography on silica gel, eluting with a 20/80 and then 30/70 mixture of ethyl acetate and cyclohexane, 0.383 g of product is obtained in the form of a yellow paste.
  • step 1.5 The process is performed as described in Example 1 (step 1.5). Starting with 0.380 g (0.95 mmol) of ethyl[ ⁇ 3-[1-(1-isoquinolyl)-4-piperidyl]propyl ⁇ -amino)carbonyl]oxyacetate, obtained in step 2.5, and 4.8 ml (9.51 mmol) of a solution (2M) of methylamine in tetrahydrofuran, and after chromatography on silica gel, eluting with a 98/2 and then 95/5 mixture of dichloromethane and methanol, 0.277 g of product is obtained in the form of an oil. This oily residue is then taken up in a solution of hydrochloric acid (5N) in isopropanol and the salt formed is filtered off and then washed with ethyl acetate.
  • 5N hydrochloric acid
  • Example 2 The process is performed as described in Example 2 (step 2.1). Starting with 25.6 g (113.90 mmol) of 1-bromo-3-(trifluoromethyl)benzene, 17.66 g (136.60 mmol) of 2-(4-piperidyl)ethanol, 26.24 g (273 mmol) of sodium tert-butoxide, 2.12 g (3.41 mmol) of BINAP and 1.04 g (1.14 mmol) of tris-(dibenzylideneacetone)dipalladium, and after chromatography on silica gel, eluting with a 25/75 mixture of ethyl acetate and cyclohexane, 17.90 g of an orange-coloured oily residue are obtained.
  • a solution of 1 g (8.78 mmol) of mesyl chloride in 5 ml of dichloromethane is added dropwise under an inert atmosphere to a solution of 2 g (7.32 mmol) of 2- ⁇ 1-[3-(trifluoromethyl)phenyl]-4-piperidyl ⁇ ethanol, obtained in step 3.1, and 1.53 ml (10.98 mmol) of triethylamine in 40 ml of dichloromethane, cooled to about 0° C. Stirring is continued at 0° C. for 1 hour and then at room temperature for 2 hours.
  • the mixture is concentrated under reduced pressure.
  • the residue is taken up in dichloromethane and water, the aqueous phase is separated out and extracted twice with dichloromethane, and the combined organic phases are washed with saturated aqueous sodium chloride solution and dried over sodium sulfate. After evaporating off the solvent, the residue obtained is purified by chromatography on silica gel, eluting with a 20/80 and then 40/60 mixture of ethyl acetate and cyclohexane.
  • the residue obtained is purified by chromatography on silica gel, eluting with a 97/3 and then 95/5 mixture of dichloromethane and methanol, followed by recrystallization from a mixture of ethyl acetate and diisopropyl ether.
  • reaction mixture is allowed to cool to room temperature and is then taken up in chloroform and saturated aqueous sodium hydrogen carbonate solution.
  • the aqueous phase is separated out and extracted twice with chloroform, the combined organic phases are washed with saturated aqueous sodium chloride solution and dried over sodium sulfate, and the filtrate is concentrated under reduced pressure.
  • step 3.2 The process is performed as in Example 3 (step 3.2). Starting with 0.661 g (3 mmol) of 2-[1-(6-methyl-2-pyridyl)-4-piperidyl]ethanol, obtained in step 4.1, 0.378 g (3.30 mmol) of mesyl chloride and 0.63 ml (4.50 mmol) of triethylamine, 0.779 g of product is obtained in the form of an orange-coloured oil, which is used without further purification in the following step.
  • step 3.3 The process is performed according to the method described in Example 3 (step 3.3). Starting with 0.776 g (2.60 mmol) of 2-[1-(6-methyl-2-pyridyl)-4-piperidyl]ethyl methanesulfonate, obtained in step 4.2, 0.315 g (3.12 mmol) of 1,3-oxazolidine-2,4-dione and 0.65 ml (5.20 mmol) of 1,1,3,3-tetramethylguanidine, and after chromatography on silica gel, eluting with a 30/70 mixture of ethyl acetate and cyclohexane, 0.76 g of pure product is obtained in the form of a yellow oil.
  • step 1.5 The process is performed according to the procedure described in Example 1 (step 1.5). Starting with 0.841 g (2.77 mmol) of 3- ⁇ 2-[1-(6-methyl-2-pyridyl)-4-piperidyl]ethyl ⁇ -1,3-oxazolidine-2,4-dione, obtained in step 4.3, and 6.9 ml (13.86 mmol) of a solution (2M) of methylamine in tetrahydrofuran, 0.598 g of pure product is obtained in the form of an oil, after chromatography on silica gel, eluting with a 95/5 mixture of dichloromethane and methanol. This oily residue is then taken up with a solution of hydrochloric acid (5N) in isopropanol and the salt formed is filtered off and then washed successively with acetone and then with ether.
  • 5N hydrochloric acid
  • Example 2 The process is performed as described in Example 2 (step 2.1). Starting with 2.50 g (15.28 mmol) of 1-chloroisoquinoline, 1.94 g (136.6 mmol) of 4-piperidylmethanol, 3.53 g (36.67 mmol) of sodium tert-butoxide, 0.285 g (0.46 mmol) of BINAP and 0.140 g (0.15 mmol) of tris(dibenzylideneacetone)dipalladium, and after chromatography on silica gel, eluting with a 98/2/0.2 and then 95/5/0.5 mixture of dichloromethane, methanol and 28% aqueous ammonia, 2.40 g of pure product are obtained in the form of a viscous orange oil.
  • a solution of 2.01 g (9.95 mmol) of diisopropyl azodicarboxylate (DIAD) in 5 ml of tetrahydrofuran is added dropwise, under an inert atmosphere, to a solution of 2.4 g (9.95 mmol) of [1-(1-isoquinolyl)-4-piperidyl]methanol, prepared in step 5.1, 2.87 g (10.94 mmol) of triphenylphosphine and 1.21 g (11.93 mmol) of 1,3-oxazolidine-2,4-dione in 40 ml of tetrahydrofuran, cooled to about ⁇ 10° C., the temperature of the reaction medium being maintained throughout between ⁇ 10° C. and 0° C. Stirring is then continued at 0° C. for 1 hour and then at 25° C. for 18 hours.
  • DIAD diisopropyl azodicarboxylate
  • the mixture is concentrated under reduced pressure and the residue is taken up in dichloromethane and 10 ml of aqueous 5% sodium hydroxide solution.
  • the aqueous phase is separated out and then extracted twice with dichloromethane.
  • the organic phases are combined and washed successively with aqueous hydrochloric acid solution (1N) and then with saturated aqueous sodium hydrogen carbonate solution and with saturated aqueous sodium chloride solution.
  • the organic phase is dried over sodium sulfate and the filtrate is concentrated under reduced pressure.
  • the residue thus obtained is purified by chromatography on silica gel, eluting with a 99/1/0.1 and then 98/2/0.2 mixture of dichloromethane, methanol and 28% aqueous ammonia.
  • step 1.5 The process is performed according to the procedure described in Example 1 (step 1.5). Starting with 3.57 g (10.97 mmol) of 3- ⁇ [1-(1-isoquinolyl)-4-piperidyl]methyl ⁇ -1,3-oxazolidine-2,4-dione, obtained in step 5.2, and 27 ml (54.86 mmol) of a solution (2M) of methylamine in tetrahydrofuran, and after chromatography on silica gel, eluting with a 95/5/0.5 mixture of dichloromethane, methanol and 28% aqueous ammonia, 0.90 g of pure product is obtained in the form of a yellow paste. This residue is then taken up in a solution of hydrochloric acid (5N) in isopropanol, and the salt formed is filtered off and then washed with acetone.
  • 5N hydrochloric acid
  • step 4.1 The process is performed as described in Example 4 (step 4.1). Starting with 1.52 g (8.39 mmol) of 1-chloro-6-fluoroisoquinoline and 1.20 g (9.23 mmol) of 2-(4-piperidyl)ethanol, and after chromatography on silica gel, eluting with a 95/5/0.5 mixture of dichloromethane, methanol and 28% aqueous ammonia, 0.90 g of pure product is obtained in the form of a yellow paste.
  • step 3.2 The process is performed as described in Example 3 (step 3.2). Starting with 1.47 g (5.36 mmol) of 2-[1-(6-fluoro-1-isoquinolyl)-4-piperidyl]ethanol, obtained in step 6.1, 0.675 g (5.89 mmol) of mesyl chloride and 1.13 ml (8.04 mmol) of triethylamine, 1.80 g of product are obtained in the form of an oil, which is used without further purification in the following step.
  • step 3.3 The process is performed according to the method described in Example 3 (step 3.3).
  • 1.8 g (5.10 mmol) of 2-[1-(6-fluoro-1-isoquinolyl)-4-piperidyl]ethyl methanesulfonate obtained in step 6.2
  • 0.62 g (6.13 mmol) of 1,3-oxazolidine-2,4-dione and 1.30 ml (10.21 mmol) of 1,1,3,3-tetramethylguanidine and after chromatography on silica gel, eluting with a 40/60 mixture of ethyl acetate and cyclohexane, 1.34 g of pure product are obtained in the form of an amorphous white solid.
  • step 2.1 The process is performed according to the protocol described in Example 2 (step 2.1). Starting with 1 g (4.81 mmol) of 4-bromoisoquinoline, 0.683 g (5.29 mmol) of 2-(4-piperidyl)ethanol, 1.11 g (11.50 mmol) of sodium tert-butoxide, 0.090 g (0.144 mmol) of BINAP and 0.044 g (0.048 mmol) of tris(dibenzylideneacetone)dipalladium, and after chromatography on silica gel, eluting with a 97/3 and then 95/5 mixture of dichloromethane and methanol, 0.810 g of product is obtained in the form of a viscous green liquid.
  • step 5.2 The procedure described in Example 5 (step 5.2) is used. Starting with 0.801 g (3.12 mmol) of 2-[1-(4-isoquinolyl)-4-piperidyl]ethanol, prepared in step 7.1, 0.902 g (3.44 mmol) of triphenylphosphine, 0.379 g (3.75 mmol) of 1,3-oxazolidine-2,4-dione and 0.632 g (3.12 mmol) of diisopropyl azodicarboxylate (DIAD), and after chromatography on silica gel, eluting with a 98/2 mixture of dichloromethane and methanol, 1 g of product is obtained in the form of a green paste.
  • DIAD diisopropyl azodicarboxylate
  • step 1.5 The procedure described in Example 1 (step 1.5) is used. Starting with 1 g (2.95 mmol) of 3- ⁇ 2-[1-(4-isoquinolyl)-4-piperidyl]ethyl ⁇ -1,3-oxazolidine-2,4-dione, obtained in step 7.2, and 7.40 ml (14.73 mmol) of a solution (2M) of methylamine in tetrahydrofuran, and after chromatography on silica gel, eluting with a 95/5 mixture of dichloromethane and methanol, 0.410 g of pure product is obtained in the form of an amorphous white solid. This oily residue is then taken up in a solution of hydrochloric acid (5N) in isopropanol and the salt formed is filtered off and then washed successively with acetone and then with diisopropyl ether.
  • 5N hydrochloric acid
  • step 4.1 The process is performed as in Example 4 (step 4.1). Starting with 2 g (12.20 mmol) of 2-chloroquinoline and 1.58 g (12.20 mmol) of 2-(4-piperidyl)-ethanol, and after chromatography on silica gel, eluting with a 98/2/0.2 and then 95/5/0.5 mixture of dichloromethane, methanol and 28% aqueous ammonia, 2.36 g of pure product are obtained in the form of a pale yellow oil that crystallizes at room temperature.
  • step 5.2 The process is performed according to the procedure described in Example 5 (step 5.2). Starting with 2.22 g (8.65 mmol) of 2-[1-(2-quinolyl)-4-piperidyl]-ethanol, prepared in step 8.1, 2.50 g (9.52 mmol) of triphenylphosphine, 1.05 g (10.38 mmol) of 1,3-oxazolidine-2,4-dione and 1.75 g (8.65 mmol) of diisopropyl azodicarboxylate (DIAD), and after chromatography on silica gel, eluting with a 30/70 and then 40/60 mixture of ethyl acetate and cyclohexane, 2.63 g of product are obtained in the form of an amorphous white solid.
  • 2-[1-(2-quinolyl)-4-piperidyl]-ethanol prepared in step 8.1
  • 2.50 g (9.52 mmol) of triphenylphosphine 1.05
  • step 1.5 The process is performed according to the procedure described in Example 1 (step 1.5). Starting with 1.5 g (4.42 mmol) of 3 ⁇ 2-[1-(2-quinolyl)-4-piperidyl]ethyl-1,3-oxazolidine-2,4-dione, obtained in step 8.2, and 11 ml (22.10 mmol) of a solution (2M) of methylamine in tetrahydrofuran, and after chromatography on silica gel, eluting with a 98/2/0.2 and then 95/5/0.5 mixture of dichloromethane, methanol and 28% aqueous ammonia, followed by crystallization from ethyl acetate, 0.405 g of pure product is obtained in the form of a white solid.
  • Example 3 The process is performed according to the procedure described in Example 3 (step 3.4). Starting with 1.14 g (3.36 mmol) of 3 ⁇ 2-[1-(2-quinolyl)-4-piperidyl]-ethyl ⁇ -1,3-oxazolidine-2,4-dione, described in Example 8 (step 8.2), and 9.60 ml (67.20 mmol) of a solution (7M) of aqueous ammonia in methanol, and after chromatography on silica gel, eluting with a 95/5 mixture of dichloromethane and methanol, followed by recrystallization from ethyl acetate, 0.360 g of pure product is obtained in the form of a white solid.
  • step 4.1 The process is performed as described in Example 4 (step 4.1). Starting with 2 g (10.10 mmol) of 2,6-dichloroquinoline and 1.44 g (11.10 mmol) of 2-(4-piperidyl)ethanol, and after chromatography on silica gel, eluting with a 98/2 mixture of dichloromethane and methanol, 2.54 g of pure product are obtained in the form of a white solid.
  • step 3.2 The process is performed as described in Example 3 (step 3.2). Starting with 2.49 g (8.56 mmol) of 2-[1-(6-chloro-2-quinolyl)-4-piperidyl]ethanol, obtained in step 10.1, 1.08 g (9.42 mmol) of mesyl chloride and 1.81 ml (12.84 mmol) of triethylamine, 3.10 g of product are obtained in the form of an oil, which is used without further purification in the following step.
  • step 3.3 The process is performed according to the method described in Example 3 (step 3.3).
  • 3 g (8.13 mmol) of 2-[1-(6-chloro-2-quinolyl)-4-piperidyl]ethyl methanesulfonate obtained in step 10.2, 1.09 g (10.8 mmol) of 1,3-oxazolidine-2,4-dione and 2.30 ml (18 mmol) of 1,1,3,3-tetramethylguanidine, and after chromatography on silica gel, eluting with a 98/2 mixture of dichloromethane and methanol, 2.57 g of product are obtained.
  • step 3.4 The process is performed according to the procedure described in Example 3 (step 3.4). Starting with 1.28 g (3.42 mmol) of 3- ⁇ 2-[1-(6-chloro-2-quinolyl)-4-piperidyl]ethyl ⁇ -1,3-oxazolidine-2,4-dione, obtained in step 10.3, and 22.10 ml (154.08 mmol) of a solution (7M) of aqueous ammonia in methanol, and after crystallization from ethanol, 0.64 g of pure product is obtained in the form of a white solid.
  • step 4.1 The process is performed as described in Example 4 (step 4.1). Starting with 1 g (6.11 mmol) of 3-chloroisoquinoline and 0.869 g (6.72 mmol) of 2-(4-piperidyl)ethanol, and after chromatography on silica gel, eluting with a 98/2 mixture of dichloromethane and methanol, 0.34 g of pure product is obtained in the form of an oil.
  • step 3.2 The process is performed as described in Example 3 (step 3.2). Starting with 0.34 g (1.33 mmol) of 2-[1-(3-isoquinolyl)-4-piperidyl]ethanol, obtained in step 11.1, 0.18 g (1.59 mmol) of mesyl chloride and 0.30 ml (1.99 mmol) of triethylamine, 0.44 g of product is obtained in the form of an oil, which is used without further purification in the following step.
  • step 3.3 The process is performed according to the method described in Example 3 (step 3.3). Starting with 0.44 g (1.32 mmol) of 2-[1-(3-isoquinolyl)4-piperidyl]-ethyl methanesulfonate, obtained in step 11.2, 0.16 g (1.58 mmol) of 1,3-oxazolidine-2,4-dione and 0.30 g (2.63 mmol) of 1,1,3,3-tetramethylguanidine, and after chromatography on silica gel, eluting with a 98/2 mixture of dichloromethane and methanol, 0.25 g of product is obtained.
  • step 1.5 The process is performed according to the procedure described in Example 1 (step 1.5). Starting with 0.24 g (0.71 mmol) of 3- ⁇ 2-[1-(3-isoquinolyl)-4-piperidyl]ethyl ⁇ -1,3-oxazolidine-2,4-dione, obtained in step 11.3, and 1.8 ml (3.53 mmol) of a solution (2M) of methylamine in tetrahydrofuran, and after chromatography on silica gel, eluting with a 98/2 and then 96/4 mixture of dichloromethane and methanol, followed by crystallization from diisopropyl ether, 0.16 g of pure product is obtained in the form of a white solid.
  • 26 g of product are obtained in the form of a yellow oil, which is used without further purification in the following step.
  • a solution of 21.50 ml (82.50 mmol) of tert-butyldiphenylsilyl chloride in 15 ml of dichloromethane is added dropwise, under an inert atmosphere, to a solution of 18.4 g (75 mmol) of tert-butyl 4-hydroxy-4-(2-hydroxyethyl)-1-piperidinecarboxylate, obtained in step 12.1, and 11.60 ml (82.50 mmol) of triethylamine in 100 ml of dichloromethane, cooled to about 0° C. The mixture is allowed to warm to room temperature and stirring is then continued for 12 hours. Saturated aqueous ammonium chloride solution is added to the reaction medium.
  • the aqueous phase is separated out and extracted twice with dichloromethane, the combined organic phases are washed with saturated aqueous sodium chloride solution and dried over sodium sulfate, and the filtrate is concentrated under reduced pressure.
  • the residue thus obtained is purified by chromatography on silica gel, eluting with a 10/90 and then 20/80 mixture of ethyl acetate and cyclohexane.
  • step 3.2 The process is performed as described in Example 3 (step 3.2). Starting with 0.61 g (2.22 mmol) of 2-[4-fluoro-1-(2-quinolyl)-4-piperidyl]ethanol, obtained in step 12.6, 0.280 g (2.45 mmol) of mesyl chloride and 0.35 ml (2.45 mmol) of triethylamine, 0.80 g of product is obtained in the form of an orange-coloured oil, which is used without further purification in the following step.
  • step 3.3 The process is performed according to the method described in Example 3 (step 3.3). Starting with 0.780 g (2.22 mmol) of 2-[4-fluoro-1-(2-quinolyl)-4-piperidyl]ethyl methanesulfonate, obtained in step 12.7, 0.27 g (2.66 mmol) of 1,3-oxazolidine-2,4-dione and 0.51 g (4.43 mmol) of 1,1,3,3-tetramethylguanidine, and after chromatography on silica gel, eluting with a 99/1 mixture of dichloromethane and methanol, 0.520 g of pure product is obtained in the form of a beige-coloured solid.
  • step 1.5 The process is performed according to the procedure described in Example 1 (step 1.5). Starting with 0.52 g (1.46 mmol) of 3- ⁇ 2-[4-fluoro-1-(2-quinolyl)-4-piperidyl]ethyl ⁇ -1,3-oxazolidine-2,4-dione, obtained in step 12.8, and 3.6 ml (7.28 mmol) of a solution (2M) of methylamine in tetrahydrofuran, and after chromatography on silica gel, eluting with a 99/1 mixture of ethyl acetate and methanol, followed by crystallization from diethyl ether, 0.390 g of pure product is obtained in the form of a white solid.
  • step 4.1 The process is performed as described in Example 4 (step 4.1). Starting with 30.20 g (127 mmol) of 2,6-dibromopyridine and 16.45 g (127 mmol) of 2-(4-piperidyl)ethanol, and after chromatography on silica gel, eluting with a 30/70 mixture of ethyl acetate and cyclohexane, 7 g of pure product are obtained in the form of an oil.
  • step 3.2 The process is performed as described in Example 3 (step 3.2).
  • 7 g (24.50 mmol) of 2-[1-(6-bromo-2-pyridyl)-4-piperidyl]ethanol obtained in step 13.1
  • 2.50 ml (26.90 mmol) of mesyl chloride and 3.80 ml (26.90 mmol) of triethylamine 8.68 g of product are obtained in the form of an oil, which is used without further purification in the following step.
  • step 3.3 The process is performed according to the method described in Example 3 (step 3.3). Starting with 8.68 g (23.80 mmol) of 2-[1-(6-bromo-2-pyridyl)-4-piperidyl]ethyl methanesulfonate, obtained in step 13.2, 2.90 g (28.60 mmol) of 1,3-oxazolidine-2,4-dione and 6 ml (47.60 mmol) of 1,1,3,3-tetramethylguanidine, and after chromatography on silica gel, eluting with a 97/3 mixture of dichloromethane and methanol, 4.52 g of product are obtained in the form of an oil.
  • the reaction mixture is poured into water and ethyl acetate.
  • the phases are separated by settling, the aqueous phase is extracted twice with ethyl acetate, the combined organic phases are dried over sodium sulfate and the filtrate is concentrated under reduced pressure.
  • the residue thus obtained is purified by chromatography on silica gel, eluting with a 20/80 mixture of ethyl acetate and cyclohexane.
  • step 1.5 The process is performed according to the procedure described in Example 1 (step 1.5). Starting with 0.72 g (2.08 mmol) of 3- ⁇ 2-[1-(6-isobutyl-2-pyridyl)-4-piperidyl]ethyl ⁇ -1,3-oxazolidine-2,4-dione, obtained in step 13.4, and 5.20 ml (10.40 mmol) of a solution (2M) of methylamine in tetrahydrofuran, and after chromatography on silica gel, eluting with a 95/5/0.5 mixture of dichloromethane, methanol and 28% aqueous ammonia, followed by crystallization from diisopropyl ether, 0.540 g of pure product is obtained in the form of a white solid.
  • step 3.4 The process is performed according to the procedure described in Example 3 (step 3.4). Starting with 0.175 g (0.499 mmol) of 3- ⁇ 2-[1-(6-phenyl-2-pyridyl)-4-piperidyl]methyl ⁇ -1,3-oxazolidine-2,4-dione, obtained in step 14.1, and 2.5 ml (17.45 mmol) of a solution (7M) of aqueous ammonia in methanol, 0.070 g of pure product is obtained in the form of a white solid, after crystallization from ethyl acetate.
  • step 4.1 The process is performed as described in Example 4 (step 4.1). Starting with 4.78 g (24.14 mmol) of 2-chloro-5-chloroquinoline (J. Med. Chem., 2002, 45, 3130–3137) and 3.43 g (26.55 mmol) of 2-(4-piperidyl)ethanol, 7 g of product are obtained in the form of an oil, which is used without further purification in the following step.
  • step 3.2 The process is performed as described in Example 3 (step 3.2). Starting with 7 g (24.07 mmol) of 2-[1-(5-chloro-2-quinolyl)-4-piperidyl]ethanol, obtained in step 15.1, 3.31 g (28.89 mmol) of mesyl chloride and 5.10 ml (36.11 mmol) of triethylamine, 8.70 g of product are obtained in the form of an oil, which is used without further purification in the following step.
  • step 3.3 The process is performed according to the method described in Example 3 (step 3.3). Starting with 8.7 g (23.58 mmol) of 2-[1-(5-chloro-2-quinolyl)-4-piperidyl]ethyl methanesulfonate, obtained in step 15.2, 2.86 g (28.30 mmol) of 1,3-oxazolidine-2,4-dione and 5.43 g (47.17 mmol) of 1,1,3,3-tetramethyl-guanidine, and after chromatography on silica gel, eluting with a 99.5/0.5 mixture of dichloromethane and methanol, 6.40 g of product are obtained in the form of a white solid.
  • step 1.5 The process is performed according to the procedure described in Example 1 (step 1.5). Starting with 6.40 g (17.12 mmol) of 3- ⁇ 2-[1-(5-chloro-2-quinolyl)-4-piperidyl]ethyl ⁇ -1,3-oxazolidine-2,4-dione, obtained in step 15.3, and 60 ml (119.84 mmol) of a solution (2M) of methylamine in tetrahydrofuran, and after chromatography on silica gel, eluting with a 98/2 and then 96/4 mixture of dichloromethane and methanol, followed by crystallization from diisopropyl ether, 5.14 g of product are obtained in the form of a white solid.
  • Table 1 illustrates the chemical structures and physical properties of a number of compounds according to the invention.
  • 2 3 N (CH 2 ) 3 CH 2 CONHCH 3 base 100(dec.) 35.
  • 2 3 N (CH 2 ) 3 CH 2 CONHCH 3 HCl 451* 36.
  • 22 22 CHCH CH 2 (CH 2 ) 2 CH 2 CONH 2 CH 2 CONH 2 basebase 327*162–163 80.81.82. 222 222 CHCHCH —CH 2 (CH 2 ) 2 CH 2 CONH 2 CH 2 CONH 2 CH 2 CONH 2 basebasebase 16876174–175 83.84. 22 22 CHCH CH 2 (CH 2 ) 2 CH 2 CONH 2 CH 2 CONH 2 basebase 169–170145–146 85.86. 22 22 CHCH (CH 2 ) 2 (CH 2 ) 2 CH 2 CONH 2 CH 2 CONHCH 3 basebase 119–121109–111 87.88.
  • 22 22 CHCH CH 2 (CH 2 ) 2 CH 2 CONH 2 CH 2 CONH 2 basebase 169–170164–165 89. 2 2 CH CH 2 CH 2 CONH 2 base 174–175 90.91. 22 22 CHCH CH 2 (CH 2 ) 2 CH 2 CONH 2 CH 2 CONH 2 basebase 162–163151–152 92.93. 22 22 CHCH —CH 2 CH 2 CONH 2 CH 2 CONH 2 basebase 195–196229–230 94.95.96. 222 222 CHCHCH —CH 2 (CH 2 ) 2 CH 2 CONH 2 CH 2 CONH 2 basebasebase 194–195222–223182 97.98.
  • 22 22 CHCH (CH 2 ) 2 (CH 2 ) 2 CH 2 CONH 2 CH 2 CONHCH 3 basebase 196–199161–163 99.100. 22 22 CHCH CH 2 (CH 2 ) 2 CH 2 CONH 2 CH 2 CONH 2 basebase 157–158175–176 101. 2 2 CH CH 2 CH 2 CONH 2 base 163–164 102. 2 2 CH (CH 2 ) 2 CH 2 CONH 2 base 418* 103. 2 2 CH CH 2 CH 2 CONH 2 base 190–191 104. 2 2 CH (CH 2 ) 2 CH 2 CONH 2 base 165–166 105.106. 22 22 CHCH CH 2 (CH 2 ) 2 CH 2 CONH 2 CH 2 CONH 2 basebase 323*202–203 107.
  • 22 22 CHCH CH 2 (CH 2 ) 2 CH 2 CONH 2 CH 2 CONH 2 basebase 161–162126–127 118.119. 22 22 CHCH CH 2 (CH 2 ) 2 CH 2 CONH 2 CH 2 CONH 2 basebase 158–159174–175 120. 2 CH (CH 2 ) 2 CH 2 CONH 2 base 204–205 121.122. 22 22 CHCH CH 2 (CH 2 ) 2 CH 2 CONH 2 CH 2 CONH 2 basebase 229–230228–229 123.124.125.126.127.128.129.
  • the compounds of the invention underwent pharmacological trials to determine their inhibitory effect on the enzyme FAAH (Fatty Acid Amide Hydrolase).
  • the enzymatic reaction is then performed in 70 ⁇ l of buffer containing fatty-acid-free bovine serum albumin (1 mg/ml).
  • anandamide[ethanolamine 1- 3 H] (specific activity of 15–20 Ci/mmol) diluted to 10 ⁇ M with cold anandamide, and the membrane preparation (400 ⁇ g of frozen tissue per test) are successively added.
  • the enzymatic reaction is quenched by adding 140 ⁇ L of chloroform/methanol (2:1). The mixture is stirred for 10 minutes and then centrifuged for 15 minutes at 3500 g.
  • Table 2 shows the IC 50 values of a few compounds according to the invention.
  • the compounds according to the invention have inhibitory activity on the enzyme FAAH.
  • the in vivo activity of the compounds of the invention was evaluated in a test of analgesia.
  • PBQ phenylbenzoquinone, 2 mg/kg in 0.9% sodium chloride solution containing 5% ethanol
  • the test compounds are administered orally or intraperitoneally as a 0.5% suspension in Tween 80, 60 minutes or 120 minutes before the administration of PBQ.
  • the most powerful compounds of the invention produce a 35% to 70% reduction in the number of tractions induced with PBQ, within a dose range of between 1 and 30 mg/kg.
  • Table 3 shows the results of the analgesia test for a few compounds according to the invention.
  • the enzyme FAAH (Chemistry and Physics of Lipids, (2000), 108, 107–121) catalyses the hydrolysis of the endogenous amide and ester derivatives of various fatty acids such as N-arachidonoylethanolamine (anandamide), N-palmitoylethanolamine, N-oleoylethanolamine, oleamide or 2-arachidonoylglycerol. These derivatives exert different pharmacological activities by interacting, inter alia, with the cannabinoid and vanilloid receptors.
  • the compounds of the invention block this degradation pathway and increase the tissue content of these endogenous substances. They may be used in this respect in the prevention and treatment of pathologies in which the endogenous cannabinoids, and/or any other substrates metabolized by the enzyme FAAH, are involved. Examples that may be mentioned include the following diseases and complaints:
  • a subject of the invention is also medicinal products comprising a compound of formula (I), or an acid-addition salt, or alternatively a pharmaceutically acceptable hydrate or solvate of the compound of formula (I). These medicinal products find their therapeutic use especially in the treatment of the pathologies mentioned above.
  • the present invention relates to pharmaceutical compositions containing, as active principal, at least one compound according to the invention.
  • These pharmaceutical compounds contain an effective dose of a compound according to the invention, or a pharmaceutically acceptable acid-addition salt, hydrate or solvate of the said compound, and optionally one or more pharmaceutically acceptable excipients.
  • excipients are chosen, according to the pharmaceutical form and the desired administration form, from the usual excipients known to those skilled in the art.
  • compositions of the present invention for oral, sublingual, subcutaneous, intramuscular, intravenous, topical, local, intrathecal, intranasal, transdermal, pulmonary, ocular or rectal administration may be administered in a unit administration form, as a mixture with standard pharmaceutical excipients, to man and animals for the prophylaxis or treatment of the above disorders or diseases.
  • the appropriate unit administration forms comprise oral forms such as tablets, soft or hard gel capsules, powders, granules, chewing gums and oral solutions or suspensions, sublingual, buccal, intratracheal, intraocular and intranasal administration forms, forms for administration by inhalation, subcutaneous, intramuscular or intravenous administration forms and rectal or vaginal administration forms.
  • oral forms such as tablets, soft or hard gel capsules, powders, granules, chewing gums and oral solutions or suspensions
  • sublingual, buccal, intratracheal intraocular and intranasal administration forms
  • forms for administration by inhalation subcutaneous, intramuscular or intravenous administration forms and rectal or vaginal administration forms.
  • the compounds according to the invention may be used in creams, ointments or lotions.
  • a unit administration form of a compound according to the invention in the form of a tablet may comprise the following components:
  • the said unit forms are dosed to allow a daily administration of from 0.01 to 20 mg of active principal per kg of body weight, depending on the presentation form.
  • the dose that is suitable for each patient is determined by the doctor according to the mode of administration and the weight and response of the said patient.
  • the invention also relates to a method for treating the pathologies mentioned above, which comprises the administration of an effective dose of a compound according to the invention, a pharmaceutically acceptable acid-addition salt thereof or a solvate or hydrate of the said compound.

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Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20080089845A1 (en) * 2006-09-07 2008-04-17 N.V. Organon Methods for determining effective doses of fatty acid amide hydrolase inhibitors in vivo
US20080119549A1 (en) * 2006-11-20 2008-05-22 N.V. Organon Metabolically-stabilized inhibitors of fatty acid amide hydrolase
US20090099240A1 (en) * 2006-10-02 2009-04-16 N.V. Organon Methods for treating energy metabolism disorders by inhibiting fatty acid amide hydrolase activity

Families Citing this family (28)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB2397067B (en) * 2002-12-23 2005-05-11 Destiny Pharma Ltd Porphin & azaporphin derivatives with at least one cationic-nitrogen-containing meso-substituent for use in photodynamic therapy & in vitro sterilisation
FR2864080B1 (fr) 2003-12-23 2006-02-03 Sanofi Synthelabo Derives de 1-piperazine-et-1-homopiperazine-carboxylates, leur preparation et leur application en therapeutique
FR2866884B1 (fr) * 2004-02-26 2007-08-31 Sanofi Synthelabo Derives d'aryl-et d'heteroaryl-piperidinecarboxylates, leur preparation et leur application en therapeutique
FR2866885B1 (fr) 2004-02-26 2007-08-31 Sanofi Synthelabo Derives de piperidinylalkylcarbamates, leur prepation et leur application en therapeutique
FR2866888B1 (fr) 2004-02-26 2006-05-05 Sanofi Synthelabo Derives de alkylpiperazine- et alkylhomopiperazine- carboxylates, leur preparation et leur application en therapeutique
FR2866886B1 (fr) * 2004-02-26 2007-08-31 Sanofi Synthelabo Derives d'aryl-et d'heteroaryl-akylcarbamates, leur preparation et leur application en therapeutique
GB2415372A (en) 2004-06-23 2005-12-28 Destiny Pharma Ltd Non photodynamical or sonodynamical antimicrobial use of porphyrins and azaporphyrins containing at least one cationic-nitrogen-containing substituent
TW200633990A (en) 2004-11-18 2006-10-01 Takeda Pharmaceuticals Co Amide compound
EP2937341B1 (en) 2004-12-30 2017-07-05 Janssen Pharmaceutica N.V. 4-(benzyl)-piperazine-1-carboxylic acid phenylamide derivatives and related compounds as modulators of fatty acid amide hydrolase (faah) for the treatment of anxiety, pain and other conditions
FR2885364B1 (fr) * 2005-05-03 2007-06-29 Sanofi Aventis Sa Derives d'alkyl-, alkenyl-et alkynylcarbamates, leur preparation et leur application en therapeutique
PE20070099A1 (es) * 2005-06-30 2007-02-06 Janssen Pharmaceutica Nv N-heteroarilpiperazinil ureas como moduladores de la amida hidrolasa del acido graso
EP1903037A1 (de) * 2006-09-07 2008-03-26 Bayer Schering Pharma Aktiengesellschaft 1-(Het)aryl-3-[hetaryl-piperidin-4-yl]-thioharnstoffe als Modulatoren des EP2-Rezeptors
TWI434842B (zh) * 2008-07-14 2014-04-21 Astellas Pharma Inc Azole compounds
FR2934265B1 (fr) * 2008-07-23 2010-07-30 Sanofi Aventis Derives de carbamates d'alkylthiazoles, leur preparation et leur application en therapeutique
FR2938537B1 (fr) * 2008-11-14 2012-10-26 Sanofi Aventis Derives de carbamates d'alkyl-heterocycles, leur preparation et leur application en therapeutique.
FR2941696B1 (fr) * 2009-02-05 2011-04-15 Sanofi Aventis Derives d'azaspiranyl-alkylcarbamates d'heterocycles a 5 chainons, leur preparation et leur application en therapeutique
RU2549547C2 (ru) * 2009-04-22 2015-04-27 Янссен Фармацевтика Нв Азетидинилдиамиды в качестве ингибиторов моноацилглицерин-липазы
FR2945531A1 (fr) * 2009-05-12 2010-11-19 Sanofi Aventis Derives de 7-aza-spiro°3,5!nonane-7-carboxylates, leur preparation et leur application en therapeutique
WO2011029633A1 (en) * 2009-09-14 2011-03-17 Recordati Ireland Limited Heterocyclic mglu5 antagonists
WO2011085216A2 (en) 2010-01-08 2011-07-14 Ironwood Pharmaceuticals, Inc. Use of faah inhibitors for treating parkinson's disease and restless legs syndrome
US20130224151A1 (en) 2010-03-31 2013-08-29 United States Of America Use of FAAH Inhibitors for Treating Abdominal, Visceral and Pelvic Pain
UA108233C2 (uk) 2010-05-03 2015-04-10 Модулятори активності гідролази амідів жирних кислот
GB201017345D0 (en) 2010-10-14 2010-11-24 Proximagen Ltd Receptor antagonists
LT2800565T (lt) * 2012-01-06 2020-07-27 Lundbeck La Jolla Research Center, Inc. Karbamato junginiai ir jų gamybos būdai ir panaudojimai
DE102012018115A1 (de) 2012-09-13 2014-03-13 Matthias Lehr Aryl-N-(arylalkyl)carbamate als Hemmstoffe der Fatty Acid Amide Hydrolase
US9828352B2 (en) 2013-07-18 2017-11-28 Fondazione Istituto Italiano Di Tecnologia Phenyl carbamates and their use as inhibitors of the fatty acid amide hydrolase (FAAH) enzyme and modulators of the D3 dopamine receptor (D3DR)
DE102013016573A1 (de) 2013-10-04 2015-04-09 Matthias Lehr 1-Tetrazolylpropan-2-one als Inhibitoren von cytosolischer Phospholipase A2 und Fatty Acid Amide Hydrolase, insbesondere geeignet zur topischen Anwendung
CN107438437B (zh) 2015-04-02 2021-01-01 普罗克斯马根有限责任公司 用于癌症的治疗

Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4539323A (en) 1982-09-25 1985-09-03 Boehringer Ingelheim Kg N-[1-(4-Amino-6,7-dialkoxy-2-quinazolinyl)-4-piperidyl]-oxazolidine-2,4-diones
WO1998043636A1 (fr) 1997-03-28 1998-10-08 Sanofi-Synthelabo Composition pharmaceutique pour administration orale d'un derive du n-piperidino-3-pyrazolecarboxamide, de ses sels et de leurs s olvates
WO2001064632A1 (fr) 2000-03-03 2001-09-07 Aventis Pharma S.A. Derives d'azetidine, leur preparation et les compositions pharmaceutiques les contenant

Family Cites Families (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR2783246B1 (fr) * 1998-09-11 2000-11-17 Aventis Pharma Sa Derives d'azetidine, leur preparation et les medicaments les contenant
FR2816938B1 (fr) 2000-11-22 2003-01-03 Sanofi Synthelabo Derives de 3-aroylindole, leur procede de preparation et les compositions pharmaceutiques en contenant
FR2843964B1 (fr) * 2002-08-29 2004-10-01 Sanofi Synthelabo Derives de dioxane-2-alkylcarbamates, leur preparation et leur application en therapeutique

Patent Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4539323A (en) 1982-09-25 1985-09-03 Boehringer Ingelheim Kg N-[1-(4-Amino-6,7-dialkoxy-2-quinazolinyl)-4-piperidyl]-oxazolidine-2,4-diones
WO1998043636A1 (fr) 1997-03-28 1998-10-08 Sanofi-Synthelabo Composition pharmaceutique pour administration orale d'un derive du n-piperidino-3-pyrazolecarboxamide, de ses sels et de leurs s olvates
WO2001064632A1 (fr) 2000-03-03 2001-09-07 Aventis Pharma S.A. Derives d'azetidine, leur preparation et les compositions pharmaceutiques les contenant

Non-Patent Citations (7)

* Cited by examiner, † Cited by third party
Title
Beringue et al., CA 126:324757, 1997. *
Brittain, "Polymorphism in Pharmaceutical Solids", 1999, pp. 5-8. *
Cecil, "Textbook of Medicine", 1982, pp. 1397-1401. *
Grever et al., Seminars in Oncology, 19(6), 1992, 622-629. *
Heinonen, "Current Atherosclerosis Reports", 2002, 4(1), summary. *
Thomas et al., Archives de Maladies du Coeur et des Vaisseaux, 1992, 85, III, summary. *
Tomlinson et al., CA 127:174580, 1997. *

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20080089845A1 (en) * 2006-09-07 2008-04-17 N.V. Organon Methods for determining effective doses of fatty acid amide hydrolase inhibitors in vivo
US20090099240A1 (en) * 2006-10-02 2009-04-16 N.V. Organon Methods for treating energy metabolism disorders by inhibiting fatty acid amide hydrolase activity
US20080119549A1 (en) * 2006-11-20 2008-05-22 N.V. Organon Metabolically-stabilized inhibitors of fatty acid amide hydrolase

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